CN112358996B - Lactobacillus casei for improving quality of paper mulberry silage and application thereof - Google Patents
Lactobacillus casei for improving quality of paper mulberry silage and application thereof Download PDFInfo
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Abstract
The lactobacillus casei is preserved in the China general microbiological culture Collection center of the China Committee for culture Collection of microorganisms, has the preservation date of 2020, 8 months and 17 days, and has the preservation number of CGMCC NO. 20432. The mixed microbial inoculum of the lactobacillus casei and the strains CGMCC NO.13132 and CGMCC NO.16062 is used for carrying out ensiling fermentation on broussonetia papyrifera to prepare ensiling feed. The lactobacillus casei provided by the invention has high cooperativity, inhibits harmful bacteria, generates a large amount of lactic acid and quickly reduces the pH value of a fermentation material. The strain is used in broussonetia papyrifera silage after being compounded and combined with two strains of CGMCC NO.13132 and CGMCC NO.16062, can quickly generate lactic acid, quickly reduce the pH value of the broussonetia papyrifera silage, inhibit the growth and the reproduction of harmful microorganisms, improve the quality of the broussonetia papyrifera silage, improve the nutritional value and the palatability of the feed, and has the advantages of simple application and low cost.
Description
Technical Field
The invention belongs to the technical field of microbial fermentation feed, and particularly relates to lactobacillus casei for improving the silage quality of paper mulberry and application thereof.
Background
The shortage of protein feed resources and high-quality coarse feed resources is a main factor for restricting the development of the animal husbandry in China, and the development of new forage grass resources is an important solution for coping with the development of the animal husbandry in China. The paper mulberry is a special mulberry deciduous tree in the mulberry family in China, and has the characteristics of high growth speed, strong stress resistance, drought resistance, salt and alkali resistance and the like, the crude protein content of the whole plant can reach 20%, and the protein content of leaves is 1.4 times of the protein content of alfalfa. However, the paper mulberry is accumulated more in rainy season, and the water content is up to 70%, so that the paper mulberry is inconvenient for long-term storage, and the paper mulberry is more suitable for long-term storage and utilization by adopting the ensiling technology.
Ensiling is a method for creating a closed anaerobic environment by sealing and compacting, producing organic acids such as lactic acid through lactic acid bacteria fermentation, rapidly reducing pH, and inhibiting the growth, metabolism and reproduction of other microorganisms, thereby reducing the loss of nutrient substances of paper mulberry raw materials, protecting feeds from being invaded by harmful microorganisms, improving the palatability of the feeds, and enabling the feeds to be stored for a long time. However, the broussonetia papyrifera leaves have villi on both surfaces, so that the broussonetia papyrifera leaves are easy to adsorb sundry bacteria in the air, the quantity of lactic acid bacteria attached to the raw materials is small, the buffering capacity is high, and the like, so that the broussonetia papyrifera ensiling effect is poor. In order to solve the problem of silage failure caused by few lactic acid bacteria and many other bacteria in the paper mulberry raw material, an additional lactic acid bacteria agent is needed, however, the silage effect of the paper mulberry cannot be improved by adding conventional commercial lactic acid bacteria, and a lactobacillus casei additive special for paper mulberry silage is not reported.
Disclosure of Invention
In order to solve the technical problems, the invention provides the lactic acid bacteria strain for improving the quality of paper mulberry silage, and the lactic acid bacteria strain has high cooperativity, inhibits harmful bacteria, generates a large amount of lactic acid and quickly reduces the pH value of a fermented material.
In order to achieve the purpose, the invention adopts the following technical scheme that:
the lactobacillus casei for improving the quality of the broussonetia papyrifera silage is preserved in the common microorganism center of China Committee for culture Collection of microorganisms, the preservation date is 2020, 08 and 17 days, and the preservation number is CGMCC NO. 20432.
The compound lactobacillus ensiling agent comprises lactobacillus casei with the number of CGMCC NO.20432, lactobacillus plantarum with the number of CGMCC NO.13132 and enterococcus faecalis with the number of CGMCC NO. 16062.
The compound silage bacterial agent is preferably the strain CGMCC NO. 13132: CGMCC NO. 20432: the inoculation ratio of CGMCC NO.16062 is 0.5:2:0.5 according to the volume ratio.
Preferably, the bacterial concentrations of the strains CGMCC NO.13132 and CGMCC NO.20432 are respectively more than or equal to 108CFU/mL, the concentration of the bacteria of CGMCC NO.16062 is more than or equal to 107CFU/mL。
The lactobacillus casei for improving the silage quality of the paper mulberry is applied to the preparation of silage, and preferably, the lactobacillus casei and mixed microbial inoculum of the strains CGMCC NO.13132 and CGMCC NO.16062 are used for carrying out silage fermentation on the paper mulberry to prepare the silage.
As mentioned above, preferably, the Lactobacillus casei is mixed with the strains CGMCC NO.13132 and CGMCC NO.16062 in a volume ratio of 2:0.5: 0.5.
In the above application, preferably, the bacterial concentrations of the lactobacillus casei and the strains CGMCC NO.13132 and CGMCC NO.20432 are respectively more than or equal to 108CFU/mL, the concentration of the bacteria of CGMCC NO.16062 is more than or equal to 107CFU/mL。
In the application, preferably, the mixed microbial inoculum is added into the branches and leaves of the paper mulberry according to the weight ratio of 1-2% of the total volume of fresh branches and leaves of the paper mulberry, molasses accounting for 2-5% of the mass of the branches and leaves of the paper mulberry is added, the mixture is uniformly stirred and then placed into a breathing bag for compaction and sealing, and the fermentation temperature is 25-35 ℃ for ensiling for 40-50 days.
Wherein the volume weight ratio is mL/g, 1-2% of 100g is added with 1-2 mL of bacterial liquid.
In the application, the length of the fresh broussonetia papyrifera branches and leaves is preferably 1-2 cm.
The invention has the beneficial effects that:
the lactobacillus casei for improving the quality of paper mulberry silage provided by the invention has the advantages of high cooperativity, inhibition of harmful bacteria, generation of a large amount of lactic acid, reduction of the pH value of a fermentation material and the like. The screened strains are compounded to be used as a broussonetia papyrifera ensiling lactobacillus inoculant and are compounded and combined with two strains of CGMCC NO.13132 and CGMCC NO.16062 of the China Committee for culture Collection of microorganisms, so that the broussonetia papyrifera ensiling lactobacillus inoculation agent can be used in broussonetia papyrifera ensiling feed, can quickly generate lactic acid, quickly reduce the pH value of the broussonetia papyrifera ensiling feed, inhibit the growth and the propagation of harmful microorganisms, improve the quality of broussonetia papyrifera ensiling, improve the nutritional value and the palatability of the feed, and has the advantages of simple application and low cost.
Drawings
FIG. 1 is a microscopic view of gram stain of the screened strain;
FIG. 2 is an electrophoretogram of 16S rDNA amplified from three selected strains;
FIG. 3 shows the growth curves of three lactic acid bacteria.
Detailed Description
The following examples are intended to further illustrate the invention but should not be construed as limiting it. Modifications and substitutions may be made thereto without departing from the spirit and scope of the invention.
Unless otherwise specified, the technical means used in the examples are conventional means well known to those skilled in the art.
Example 1 screening of Special species for Broussonetia papyrifera silage
1) Liquid enrichment: selecting a paper mulberry ensiling sample with pH of 4.0-4.5, putting 3-5g of the sample into a sterilized 100mL MRS liquid culture medium, and performing static culture for 36-48 h in an incubator at 37 ℃. Wherein the MRS liquid culture medium comprises 2 percent of sucrose, 1 percent of peptone, 1 percent of beef extract, 0.5 percent of yeast extract powder, 0.5 percent of sodium acetate, 0.2 percent of ammonium citrate and 0.2 percent of K in percentage by mass2HPO4、0.05％MgSO4·7H2O、0.02％MnSO4·4H2O, 0.1% Tween and the balance of water, and the pH is adjusted to 6.2-6.4.
2) Solid culture: sucking 1mL of the liquid-enriched bacterial liquid, and performing the sucking with physiological saline 10%-4、10-5、10-6Gradient dilution, sucking 200 μ L of diluent, uniformly plating on MRS solid culture medium, standing in 37 deg.C incubator for 36-48 h, selecting colony with good colony morphology and good growth condition, streaking and purifying in MRS solid culture medium, and culturing with the same stripRepeating the steps for 5-6 times respectively. Wherein, the solid medium has the same components as the liquid medium in the step 1, except that 2 percent agar powder is additionally added.
3) Separation and purification: respectively culturing 20 strains by solid culture for 10 times-4、10-5、10-6And (3) three gradient dilutions, namely respectively taking 100 mu L of diluted bacterial liquid, coating the diluted bacterial liquid in a calcium carbonate selective culture medium, performing static culture in an incubator at 37 ℃ for 36-48 h, comparing the diameter of a bacterial colony with the diameter of a hydrolysis ring, wherein the larger the diameter of the hydrolysis ring is, the stronger the acid production capacity of the bacterial strain is, and the result is shown in table 1. Wherein, the solid culture medium has the same components as the liquid culture medium in the step 1, and 2 percent of calcium carbonate is additionally added.
4) And (3) gram staining observation: and dipping the bacterial liquid by using a sterilized inoculating loop, placing the bacterial liquid on a clean glass slide, performing slide production and gram staining on the strains, and comparing morphological changes of the separated 20 strains. The results are shown in Table 1, 17 bacterial smears of the 20 selected strains are gram-positive bacteria which show blue-purple, the strains are observed to be short rods or chains under a microscope, and the test results are shown in FIG. 1.
5) Catalase assay: and dipping the bacterial liquid by using a sterilized inoculating loop, coating the bacterial liquid on a clean glass slide, and dropwise adding 30% hydrogen peroxide, wherein if bubbles are generated, the hydrogen peroxide test is positive, and otherwise, the hydrogen peroxide test is negative. The experimental result shows that the catalase tests of the selected strains are positive and are identified as the bacteria of the genus Lactobacillus.
TABLE 1 lactic acid bacteria identification physiological and biochemical experiments
Remarking: + indicates bluish purple gram staining, -negative result of hydrogen peroxide test, and/indicates no detection.
6)16S rDNA strain identification: through gram staining and catalase experiments, three lactic acid bacteria BFEC-6, BFEC-7 and BFEC-18 with large colony diameter and strong acid production capability are comprehensively bred for agar gel electrophoresis analysis. Extracting gene DNA by using a bacterial genome DNA extraction kit, and amplifying a bacterial 16 SR DNA sequence by PCR, wherein an upstream primer P1 and a downstream primer P2 of a PCR primer sequence of a strain are respectively:
P1(SEQ ID No.1)：5’-AGAGTTTGATCCTGGCTCAG-3’；
P2(SEQ ID No.2)：5’-GGTTACCTTGTTACGACTT-3’；
after the PCR circulation is finished, the PCR products are analyzed by 0.1% agarose gel electrophoresis, the DNA genome extracted by the three strains is proved to accord with the bacterial genus gene fragment, and the electrophoresis detection result is shown in figure 2. The extracted DNA genome is sent to Beijing Nonsui genome research center for sequence determination.
After the PCR is amplified by the 16S r DNA primer, a PCR amplified fragment of about 1500bp is obtained. The sequence of the 16S rDNA sequencing result of the obtained strain is shown in SEQ ID No.3, Blast sequence comparison is carried out in an NCBI database, and the comparison result shows that: the similarity between the strain BFEC-7 and the lactobacillus casei is more than or equal to 97 percent, and the strain BFEC-7 is identified as the lactobacillus casei; the similarity between the strains BFEC-6 and BFEC-18 and the lactobacillus rhamnosus is more than or equal to 97 percent, and the BFEC-6 is identified as the lactobacillus rhamnosus.
And 2, identifying 17 lactobacillus strains with short rod-shaped or chain-shaped appearance through gram staining observation and catalase test, selecting three strains of BFEC-6, BFEC-7 and BFEC-18 according to the diameter of the bacterial colony and the diameter of a hydrolysis ring, and identifying the strain BFEC-7 as lactobacillus casei with large bacterial colony diameter, large transparent ring diameter and strong acid-producing capacity. The strain is numbered as BFEC2002G3, and is preserved in China general microbiological culture Collection center of China Committee for culture Collection on day 17 of 08 month 2020, wherein the preservation address is the microbiological research institute of China academy of sciences, No.3 of West Lu 1 Hospital, North Kyoto, Chaoyang, Beijing, and the classification is named: lactobacillus casei (Lactobacillus casei) with preservation number of CGMCC NO. 20432.
Example 2 probiotic Properties of Lactobacillus casei according to the invention
Respectively inoculating the separated lactobacillus casei CGMCC NO.20432(BFEC-7), lactobacillus plantarum CGMCC NO.13132 and enterococcus faecalis CGMCC NO.16062 into MRS liquid culture medium, standing and culturing in a 37 ℃ incubator, detecting absorbance every other hour from the fourth hour by using an enzyme-labeling instrument, recording the absorbance value and evaluating the growth speed of the strain. The experimental data are shown in FIG. 3. The lactobacillus plantarum with the number of CGMCC NO.13132 and the enterococcus faecalis with the number of CGMCC NO.16062 are explained in the 'livestock and poultry general composite fermentation inoculant with the application number of 201911203375.7 and the preparation method and the application thereof', and are not described herein again. The strains selected in the application are three strains which are finally selected and determined through a large number of experimental verifications.
The conclusion is that the CGMCC NO.20432 and 13132 strains have high growth speed, and the growth speed of the NO.16062 strain is obviously lower than that of the other two strains.
Three strains (CGMCC NO.13132, NO.20432 and NO.16062) are inoculated according to the volume ratio (wherein the bacterial concentrations in the CGMCC NO.13132 and NO.20432 bacterial liquids are respectively 1 multiplied by 10)8Bacterial concentration in CFU/mL, NO.16062 bacterial liquid is 1.1 × 107CFU/mL) is 1:0: 0; 0:1: 0; 0:0: 1; 1:1: 1; 0.5:2: 0.5; 0.5:0.5: 2; 2:0.5:0.5, and carrying out bacterial suspension preparation. And (3) statically culturing the bacterial suspension in an incubator at 37 ℃, detecting indexes such as pH, lactic acid and the like, and evaluating the acid production condition of the bacterial strain. The experimental data are shown in tables 2 and 3.
TABLE 2 pH of the bacterial suspension
And (4) conclusion: after the three strains are subjected to compound culture, the inoculation ratio of NO.13132, NO.20432(BFEC-7, namely BFEC2002G3) and NO.16062 is 0.5:2:0.5, the pH value of the three strains is lower than that of other treatment groups, and the pH value of the three strains is obviously lower than that of a single strain suspension.
TABLE 3 lactic acid production of bacterial suspensions (mmol/L)
The conclusion is that the lactic acid yield is the highest after the lactobacillus casei No.20432 is fermented for 48 hours; the three strains are compounded, and the lactic acid yield of the compound mixed bacterial suspension with the inoculation ratio of NO.13132, NO.20432 and NO.16062 being 0.5:2:0.5 is the highest.
Transferring the purified and mature slant lawn on the slant culture medium into MRS liquid culture medium with inoculating needle, standing and culturing at 37 deg.C for 36-48 h, and centrifuging at 4 deg.C for 10min at 8000r/min to obtain lactobacillus supernatant. The inoculation ratio of the supernatant of the three strains (NO.13132, NO.20432 and NO.16062) is 1:0:0 by volume ratio; 0:1: 0; 0:0: 1; 1:1: 1; 0.5:2: 0.5; 0.5:0.5: 2; 2:0.5:0.5, wherein the bacterial concentration of NO.13132 and NO.20432 is not less than 108The concentration of the CFU/mL NO.16062 bacteria is not less than 107CFU/mL. Quickly thawing Escherichia coli, Staphylococcus aureus and Salmonella preserved at-80 deg.C in water bath at 37-38 deg.C, inoculating 2-3% of the inoculum size in LB liquid culture medium, culturing at 37 deg.C for 18-24 hr to make the liquid culture medium contain bacteria 108-1012CFU/mL. And coating 100 mu L of the indicating bacterium liquid on the surface of an LB culture medium by adopting an Oxford cup method, placing an Oxford cup on the surface of a flat plate by using an aseptic operation method, adding 200 mu L of lactobacillus supernatant with different inoculation ratios into the Oxford cup, standing and culturing for 8h at 37 ℃, taking out and measuring the diameter of a bacteriostatic zone to evaluate the bacteriostatic effect of the strain. The results are shown in Table 4.
TABLE 4 results of in vitro bacterial inhibition (mm)
And (4) conclusion: the diameter of the lactobacillus casei bacteriostatic circle of CGMCC NO.20432 is higher than that of other two strains; the three strains are compounded, and the diameter of the inhibition zone is the largest according to the proportion of 0.5:2:0.5, which shows that the inhibition effect is the best.
Example 3 silage experiment of Broussonetia papyrifera silage special microbial inoculum
Culturing culture solution of strains CGMCC NO.13132, NO.20432 and NO.16062 (wherein the bacterial concentrations in the CGMCC NO.13132 and NO.20432 bacterial solutions are respectively 10)8The bacterial concentration in CFU/mL and NO.16062 bacterial liquid is 107CFU/mL) in a volume ratio of 0.5:2:0.5 to prepare a compound silage bacterial agent, cutting fresh branches and leaves of paper mulberry into 1-2cm in lengthAdding 1 percent of compound silage microbial inoculum into fresh branches and leaves according to the volume mass ratio (mL/g), namely adding 1.0mL of compound silage microbial inoculum into 100g of fresh branches and leaves, and adding molasses which accounts for 2-5 percent of the mass of the branches and leaves of the paper mulberry. Mixing, compacting in breathing bag, sealing, ensiling at 25-35 deg.C for 40-50 days, collecting ensilage at 0, 5, 10, 20, 30, and 40 days of ensilage experiment, detecting pH value with pH meter, and measuring lactic acid content in culture solution with high performance liquid chromatography.
Comparative example 1
The difference between the comparative example 1 and the example 3 is that the 'compound silage inoculant + molasses' is replaced by the 'distilled water with the same volume'.
Comparative example 2
Comparative example 2 differs from example 3 only in that "compounded silage inoculant + molasses" was replaced with "silage legend + molasses". (wherein the silage legend is from inner Mongolia silage science and technology Co., Ltd.) pH value was measured by using a pH meter, and the lactic acid content in the culture solution was measured by high performance liquid chromatography. The experimental data are shown in tables 5 and 6.
TABLE 5 Broussonetia papyrifera silage pH Change
TABLE 6 Broussonetia papyrifera silage lactic acid content variation (mmol/L-1)
And (4) conclusion: after silage is finished, by observing the broussonetia papyrifera feeds treated in the comparative example 1, the comparative example 2 and the example 3, the pH value of the broussonetia papyrifera silage treated in the example 3 is reduced fastest, and the yield of lactic acid is the highest after silage is 40 d. The screened composite silage bacterial agent has better effect on the silage of paper mulberry than the existing composite bacterial agent.
Sequence listing
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tacggctccg gcttcgggtg ttacaaactc tcatcgtgtg acgggcggtg tgtacatggc 60
ccgggaacgt attcaccgcg gcgtgctgat ccgcgttaac tagcgattcc gacttcgtgt 120
aggcgagttg cagccatcag tccgaactga gaatggcttt aagagattag cttgacctcg 180
cggtctcgca actcgttgta cctaccattg tagcacgtgt gtagcccagg tcatatgggg 240
catgatgatt tgacgtcatc ccgaccttcc tccggtttgt caccggcagt cttactagag 300
tgccctactg aatgctggca actagtctaa aggcttgcgc tcgttgcggg acttaaccca 360
acatctcacg acacgagctg acgacaacca tgcaccacct gtcattttgc ccccgaaggg 420
gaaacctgat ctctcaggtg atcaaaagat gtcaagacct ggtaaggttc ttcgcgttgc 480
ttcgaattaa accacatgct ccaccgcttg tgccggcgcc cgtcaaatcc tttgagtttc 540
aaccttgcgg tcgaactccc caggcggaat gcttaatgcg ttagctgcgg cactgaaggg 600
cggaaaccct ccaacaccta gcattcatcg ttaacggcat ggactaccag ggtatctaat 660
cctgttcgct acccatgctt tcgagcctca gcgtcagtta cagaccagac agccgccttc 720
gccactggtg ttcttccata tatctacgca tttcaccgct acacatggag ttccactgtc 780
ctcttctgca ctcaagtttc ccagtttccg atgcgcttcc tcggttaagc cgagggcttt 840
cacatcagac ttaaaaaacc gcctgcgctc gctttacgcc caataaatcc ggataacgct 900
tgccacctac gtattaccgc ggctgctggc acgtagttag ccgtggcttt ctggttggat 960
accgtcacgc cgacaacagt tactctgccg accattcttc tccaacaaca gagttttacg 1020
acccgaaagc cttcttcact cacgcggcgt tgctccatca gacttgcgtc cattgtggaa 1080
gattccctac tgctgcctcc cgtaggagtt tgggccgtgt ctcagtccca atgtggccga 1140
tcaacctctc agttcggcta cgtaacatcg ccttggtgag ccgttacctc accaactagc 1200
taatacgccg cgggtccatc caaaagcgat agcttgcgcc atctttcagc caagaaccat 1260
gcggttcttg gatttatgcg gtattagcat ctgtttccaa atgttatccc ccacttaagg 1320
gctggttacc cacgtcttac tcacccgtcc gccactcgtt ttaagttgaa tcacagtgca 1380
agcaccgttc atg 1393
Claims (10)
1. The lactobacillus casei for improving the quality of the broussonetia papyrifera silage is preserved in the common microorganism center of China Committee for culture Collection of microorganisms, the preservation date is 2020, 08 and 17 days, and the preservation number is CGMCC NO. 20432.
2. The compound silage bacterial agent for improving the quality of paper mulberry silage is characterized by comprising lactobacillus casei with the number of CGMCC NO.20432, lactobacillus plantarum with the number of CGMCC NO.13132 and enterococcus faecalis with the number of CGMCC NO. 16062.
3. The compound silage microbial inoculum according to claim 2, wherein the strain CGMCC NO. 13132: CGMCC NO. 20432: the inoculation ratio of CGMCC NO.16062 is 0.5:2:0.5 according to the volume ratio.
4. The compound silage microbial inoculum of claim 3, wherein the bacterial concentrations of the bacterial strains CGMCC NO.13132 and CGMCC NO.20432 are respectively more than or equal to 108CFU/mL, the concentration of the bacteria of CGMCC NO.16062 is more than or equal to 107CFU/mL。
5. Use of lactobacillus casei for improving the silage quality of paper mulberry according to claim 1 for the preparation of silage.
6. The use of claim 5, wherein the mixed microbial inoculum of lactobacillus casei and strains CGMCC NO.13132 and CGMCC NO.16062 is used for carrying out ensiling fermentation on broussonetia papyrifera to prepare silage.
7. The use according to claim 6, wherein the Lactobacillus casei is mixed with the strains CGMCC NO.13132 and CGMCC NO.16062 in a volume ratio of 2:0.5: 0.5.
8. The use according to claim 7, wherein the Lactobacillus casei has the strain CGMCC No.13132 and CGMCC No.20432 of 10 or more, respectively8CFU/mL, the concentration of the bacteria of CGMCC NO.16062 is more than or equal to 107CFU/mL。
9. The application of the broussonetia papyrifera as claimed in claim 6, wherein the mixed microbial inoculum is added into branches and leaves of broussonetia papyrifera according to 1% -2% of the total volume weight of fresh branches and leaves of the broussonetia papyrifera, molasses accounting for 2% -5% of the mass of the branches and leaves of the broussonetia papyrifera is added, the mixture is uniformly stirred and then placed into a breathing bag to be compacted and sealed, and the fermentation temperature is 25-35 ℃ for ensiling for 40-50 days.
10. The use according to claim 9, wherein the fresh broussonetia papyrifera branches and leaves are 1-2cm in length.
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